chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36935659369356597TTTG----10GENICheterozygous57432420
36935659469356597TTG---8GENICheterozygous57432422
36935672069356722AC--16GENIChomozygous59693309
36935673869356740AC--11GENICheterozygous57432428
36935752269357523AG32GENIChomozygous59611826
36935785769357858CT17GENIChomozygous60010174
36935798869357989AG12GENIChomozygous59611828
36935807669358077GGA14GENIChomozygous60010175
36935874469358745AG27GENICpossibly homozygous59611830
36935923569359236AG19GENIChomozygous59611832
36935934269359343TC38GENIChomozygous59611834
36935934869359349TG37GENIChomozygous57432440
36935943969359440AT33GENIChomozygous59611836
36935975669359757TC30GENIChomozygous59611838
36935984269359843AG20GENICpossibly homozygous59611842
36935999969360000AT27GENIChomozygous59611844
36936042569360426CG17GENIChomozygous59611846
36936065269360653TC25GENICpossibly homozygous59611848
36936122769361228A-25GENIChomozygous60010176
36936124569361246TC28GENIChomozygous59611850
36936214469362145CG20GENIChomozygous60010177
36936236469362365C-13GENICpossibly homozygous59611852
36936236569362366CT14GENIChomozygous58550234
36936254469362547TTT---20GENICpossibly homozygous58649559
36936290869362909GGA25GENIChomozygous59611854
36936315969363160AT27GENIChomozygous59611856
36936322969363230AG17GENIChomozygous59611858
36936416969364170CG33GENIChomozygous59611860
36936254569362547TT--20GENICheterozygous58593987